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Identification of serotonin 5-HT3 recognition sites by radioligand binding in NG108-15 neuroblastoma-glioma cells.

作者信息

Hoyer D, Neijt H C

机构信息

Preclinical Research, Sandoz Ltd., Basel, Switzerland.

出版信息

Eur J Pharmacol. 1987 Nov 10;143(2):291-2. doi: 10.1016/0014-2999(87)90547-4.

DOI:10.1016/0014-2999(87)90547-4
PMID:3691658
Abstract
摘要

相似文献

1
Identification of serotonin 5-HT3 recognition sites by radioligand binding in NG108-15 neuroblastoma-glioma cells.
Eur J Pharmacol. 1987 Nov 10;143(2):291-2. doi: 10.1016/0014-2999(87)90547-4.
2
Characterisation of 5-HT3 recognition sites in membranes of NG 108-15 neuroblastoma-glioma cells with [3H]ICS 205-930.用[³H]ICS 205-930对NG 108-15神经母细胞瘤-胶质瘤细胞膜中5-HT3识别位点的表征。
Naunyn Schmiedebergs Arch Pharmacol. 1988 May;337(5):493-9. doi: 10.1007/BF00182721.
3
Differential binding characteristics of agonists at 5-HT3 receptor recognition sites in NG108-15 neuroblastoma-glioma cells labelled by [3H]-(S)-zacopride and [3H]granisetron.用[3H]-(S)-扎考必利和[3H]格拉司琼标记的NG108-15神经母细胞瘤-胶质瘤细胞中5-HT3受体识别位点激动剂的差异结合特性
Biochem Pharmacol. 1993 May 25;45(10):2155-8. doi: 10.1016/0006-2952(93)90030-z.
4
Characterization of the novel 5-HT3 antagonists MDL 73147EF (dolasetron mesilate) and MDL 74156 in NG108-15 neuroblastoma x glioma cells.
Eur J Pharmacol. 1992 Aug 14;219(1):9-13. doi: 10.1016/0014-2999(92)90573-m.
5
Interaction of psychotropic drugs with central 5-HT3 recognition sites: fact or artifact?精神药物与中枢5-羟色胺3识别位点的相互作用：事实还是假象？
Eur J Pharmacol. 1989 Nov 14;171(1):137-9. doi: 10.1016/0014-2999(89)90438-x.
6
Characteristics of 5-HT3 binding sites in NG108-15, NCB-20 neuroblastoma cells and rat cerebral cortex using [3H]-quipazine and [3H]-GR65630 binding.使用[3H]-喹哌嗪和[3H]-GR65630结合法研究NG108-15、NCB-20神经母细胞瘤细胞及大鼠大脑皮层中5-HT3结合位点的特征
Br J Pharmacol. 1991 Apr;102(4):919-25. doi: 10.1111/j.1476-5381.1991.tb12277.x.
7
5-HT3 receptors in NG108-15 neuroblastoma x glioma cells: effect of the novel agonist 1-(m-chlorophenyl)-biguanide.
Neuropharmacology. 1992 Jun;31(6):561-4. doi: 10.1016/0028-3908(92)90188-u.
8
Identification of 5-HT3 binding sites in rat spinal cord synaptosomal membranes.大鼠脊髓突触体膜中5-羟色胺3受体结合位点的鉴定。
Eur J Pharmacol. 1988 Nov 1;156(2):287-90. doi: 10.1016/0014-2999(88)90335-4.
9
SR 57227A: a potent and selective agonist at central and peripheral 5-HT3 receptors in vitro and in vivo.SR 57227A：一种在体外和体内对中枢和外周5-羟色胺3受体具有强效和选择性的激动剂。
Eur J Pharmacol. 1993 Jun 24;237(2-3):299-309. doi: 10.1016/0014-2999(93)90282-m.
10
[3H]quaternised ICS 205-930 labels 5-HT3 receptor binding sites in rat brain.[3H]季铵化ICS 205 - 930标记大鼠脑中的5 - HT3受体结合位点。
Eur J Pharmacol. 1988 May 10;149(3):397-8. doi: 10.1016/0014-2999(88)90677-2.

引用本文的文献

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Risperidone compared with new and reference antipsychotic drugs: in vitro and in vivo receptor binding.利培酮与新型及参比抗精神病药物的比较：体外和体内受体结合情况
Psychopharmacology (Berl). 1996 Mar;124(1-2):57-73. doi: 10.1007/BF02245606.
2
Evidence that the atypical 5-HT3 receptor ligand, [3H]-BRL46470, labels additional 5-HT3 binding sites compared to [3H]-granisetron.与[3H] - 格拉司琼相比，非典型5 - HT3受体配体[3H] - BRL46470标记额外5 - HT3结合位点的证据。
Br J Pharmacol. 1995 Sep;116(2):1781-8. doi: 10.1111/j.1476-5381.1995.tb16663.x.
3
Gastroprokinetic properties of the benzimidazolone derivative BIMU 1, an agonist at 5-hydroxytryptamine4 and antagonist at 5-hydroxytryptamine3 receptors.
苯并咪唑酮衍生物BIMU 1的促胃动力特性，它是5-羟色胺4受体激动剂和5-羟色胺3受体拮抗剂。
Naunyn Schmiedebergs Arch Pharmacol. 1994 Apr;349(4):338-45. doi: 10.1007/BF00170878.
4
The interaction of antidepressant drugs with central and peripheral (enteric) 5-HT3 and 5-HT4 receptors.抗抑郁药物与中枢及外周（肠道）5-羟色胺3型和5-羟色胺4型受体的相互作用。
Br J Pharmacol. 1995 Mar;114(5):1017-25. doi: 10.1111/j.1476-5381.1995.tb13307.x.
5
Characterization of 5-HT3 receptors of N1E-115 neuroblastoma cells by use of the influx of the organic cation [14C]-guanidinium.利用有机阳离子[14C] - 胍的内流对N1E - 115神经母细胞瘤细胞的5 - HT3受体进行表征。
Br J Pharmacol. 1993 Feb;108(2):436-42. doi: 10.1111/j.1476-5381.1993.tb12822.x.
6
Antagonistic properties of McNeil-A-343 at 5-HT4 and 5-HT3 receptors.麦克尼尔-A-343对5-羟色胺4型和5-羟色胺3型受体的拮抗特性。
Br J Pharmacol. 1994 Nov;113(3):711-6. doi: 10.1111/j.1476-5381.1994.tb17051.x.
7
Increasing effect of ethanol on 5-HT3 receptor-mediated 14C-guanidinium influx in N1E-115 neuroblastoma cells.乙醇对N1E - 115神经母细胞瘤细胞中5 - HT3受体介导的14C - 胍盐内流的增强作用。
Naunyn Schmiedebergs Arch Pharmacol. 1995 Aug;352(2):149-56. doi: 10.1007/BF00176768.
8
Characterisation of 5-HT3 recognition sites in membranes of NG 108-15 neuroblastoma-glioma cells with [3H]ICS 205-930.用[³H]ICS 205-930对NG 108-15神经母细胞瘤-胶质瘤细胞膜中5-HT3识别位点的表征。
Naunyn Schmiedebergs Arch Pharmacol. 1988 May;337(5):493-9. doi: 10.1007/BF00182721.
9
Species variations in 5-HT3 recognition sites labeled by 3H-quipazine in the central nervous system.中枢神经系统中由3H-喹哌嗪标记的5-HT3识别位点的物种差异。
Naunyn Schmiedebergs Arch Pharmacol. 1988 Nov;338(5):472-5. doi: 10.1007/BF00179316.
10
Molecular pharmacology of 5-HT1D recognition sites: radioligand binding studies in human, pig and calf brain membranes.5-HT1D识别位点的分子药理学：人、猪和小牛脑膜的放射性配体结合研究
Naunyn Schmiedebergs Arch Pharmacol. 1988 Jun;337(6):595-601. doi: 10.1007/BF00175783.